This paper demonstrates a novel facile method for fabrication of patterned arrays of gold nanoparticles on Si/SiO2 by combining electron beam lithography and self-assembly techniques. Our strategy is to use direct-write electron beam patterning to convert nitro functionality in self-assembled monolayers of 3-(4-nitrophenoxy)-propyltrimethoxysilane to amino functionality, forming chemically well-defined surface architectures on the 100 nm scale. These nanopatterns are employed to guide the assembly of citrate-passivated gold nanoparticles according to their different affinities for amino and nitro groups. This kind of nanoparticle assembly offers an attractive new option for nanoparticle patterning a silicon surface, as relevant, for example, to biosensors, electronics, and optical devices.

Reductive rays: X‐ray photoelectron spectroscopy was employed to investigate the chemical change in self‐assembled films of 3‐(4‐nitrophenoxy)‐propyltrimethoxysilane (NPPTMS) on silicon (Si/SiO2) wafers upon X‐ray irradiation The results indicate conversion of the NO2 group into NH2. In order to confirm this, a self‐assembled multilayer of NPPTMS on silicon was subjected to reductive conditions (SnCl2/anhydrous EtOH) to convert the NO2 to the NH2 group. The graphic shows the time‐resolved X‐ray induced chemical reduction of the thin film on an SiO2 surface.

This paper describes the self-assembly of a heterosupramolecular system consisting of a tripodal [2]rotaxane adsorbed at the surface of a titanium dioxide nanoparticle. The tripodal [2]rotaxane consists of a dumbbell-shaped molecule, incorporating two electron-poor viologens, threading an electron-rich crown ether. The [2]rotaxane also incorporates a bulky tripodal linker group at one end and a bulky stopper group at the other end. The [2]rotaxane is adsorbed, via the tripodal linker group, at the surface of a titanium dioxide nanoparticle. The structure and function of the resulting hetero[2]rotaxane have been studied in detail by (1)H NMR spectroscopy and cyclic voltammetry. A key finding is that it is possible to electronically address and switch the above hetero[2]rotaxane.